79784-34-2 Usage
Uses
Used in Pharmaceutical Industry:
3,4-Difluorophenylglyoxal hydrate is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique chemical properties and reactivity make it a valuable component in the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 3,4-difluorophenylglyoxal hydrate is used as a key intermediate in the production of agrochemicals. Its ability to participate in various chemical reactions allows for the creation of effective and targeted agrochemical products.
Used in Fine Chemicals Industry:
3,4-Difluorophenylglyoxal hydrate is utilized as a reactive intermediate in the synthesis of fine chemicals. Its versatility in chemical reactions contributes to the development of high-quality specialty chemicals used in various applications.
Used in Organic Synthesis:
3,4-Difluorophenylglyoxal hydrate is used as a building block in organic synthesis. Its ability to undergo condensation, oxidation, and reduction reactions makes it a valuable compound for creating a wide range of organic compounds for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 79784-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,8 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79784-34:
(7*7)+(6*9)+(5*7)+(4*8)+(3*4)+(2*3)+(1*4)=192
192 % 10 = 2
So 79784-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F2O2/c9-6-2-1-5(3-7(6)10)8(12)4-11/h1-4H
79784-34-2Relevant academic research and scientific papers
FLUORINE CONTAINING BIOACTIVE HETEROCYCLES PART III : SYNTHESIS OF SOME NEW FLUORINE CONTAINING PHENYLGLYOXALS AND 1,2,4-TRIAZINE DERIVATIVES
Joshi, Krishna C.,Dubey, Kalpana,Dandia, Anshu
, p. 1545 - 1553 (2007/10/02)
Some medicinally important new fluorine containing phenylglyoxals have been synthesized by selenium dioxide oxidation of appropriate fluorinated acetophenones and characterized by spectrum studies.The phenylglyoxals were treated with thiosemicarbazide to give corresponding thiosemicarbazones (III) which were cyclized, in situ, to yield 5-(fluorophenyl)-1,2,4-triazine-3(2H)-thiones.The 5-(4-fluorophenyl)-1,2,4-triazine-3-(2H)-thione (IV) undergoes nucleophilic displacement when refluxed with hydrazine hydrate to give corresponding 3-hydrazino-5-(4-fluorophenyl)-1,2,4-tria zine.The hydrazino derivative reacts with fluorinated 1,3-diketones, in glacial acetic acid yielding 5-(4-fluorophenyl)-3--1,2,4-triazines (VII).All synthesized compounds have been characterized on the basis of elemental analyses, ir, pmr and 19F nmr studies.
